Recalls distributed in Washington – page 9

• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• CleverCut Product Name: Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical 25GA Backflush, VS0270.25 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical TID Pharos Illuminated Depressor, VS0801B recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Rumex Disposable Diamond Dusted ILM Elevator, 12-7523 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical I2 Injection Kit, VS0500 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Tecfen Retractable Membrane Polisher, QTPR1267-23 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical 25GA I.D.D. Internal Delivery Device, VS0250.25 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2… recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• 25GA Subretinal Injection Cannula VS0220.25 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive… recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2… recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical 1. 23GA Laser Probe Curved Cat No recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• MiniMed 780G Insulin Pump recall
  FDA February 11, 2026 · Medtronic MiniMed, Inc. · Class II
• CellMek SPS Sample Preparation System recall
  FDA February 11, 2026 · Beckman Coulter, Inc. · Class II
• Da Vinci Product Name: da Vinci X, Xi Surgical System… recall
  FDA February 11, 2026 · Intuitive Surgical, Inc. · Class II
• COULTER DxH Diluent recall
  FDA February 11, 2026 · Beckman Coulter, Inc. · Class II
• CINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA recall
  FDA February 11, 2026 · Venzu Traders LLC · Class II
• spicely ORGANIC sumac NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY… recall
  FDA February 11, 2026 · Organic Spices, Inc · Class II
• spicely ORGANIC celery salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO… recall
  FDA February 11, 2026 · Organic Spices, Inc · Class II
• spicely ORGANIC garlic salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO… recall
  FDA February 11, 2026 · Organic Spices, Inc · Class II
• Repackaged M&Ms candies, Net Wt 1.3 oz recall
  FDA February 11, 2026 · Beacon Promotions Inc · Class II
• Repackaged M&Ms Peanut candies, Net Wt 1.3 oz recall
  FDA February 11, 2026 · Beacon Promotions Inc · Class II
• JUICE from the Raw, cashew coffee milk recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, cashew milk recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, spicy lemonade recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, upbeat recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, pineapple mint recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, sweet greens recall
  FDA February 11, 2026 · Everpress Juice · Class I
• JUICE from the Raw, DETOX GREENS recall
  FDA February 11, 2026 · Everpress Juice · Class I
• WinCo Foods Deli Margherita Pizza Thin Crust, Item #67279. Net wt recall
  FDA February 11, 2026 · WinCo Foods LLC · Class II
• BEAR Implant recall
  FDA February 4, 2026 · Miach Orthopaedics · Class II
• SmartPath to dStream for XR and 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• SmartPath to dStream for 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Upgrade to MR 7700. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• MR 7700. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Elition X. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Elition S. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Ambition X. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Ambition S. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia 3.0T CX. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia 1.5T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Evolution Upgrade 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Evolution Upgrade 1.5T. Product Codes ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Conductivity Standard Solution recall
  FDA February 4, 2026 · NIPRO Technical Services, Inc. · Class II
• PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recall
  FDA February 4, 2026 · Cerapedics, Inc. · Class II